English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
 
 
DownloadE-Mail
  Near-Field scanning optical microscopy in cell biology and cytogenetics

Hausmann, M., Perner, B., Rapp, A., Wollweber, L., Scherthan, H., & Greulich, K.-O. (2006). Near-Field scanning optical microscopy in cell biology and cytogenetics. In D. J. Taatjes, & B. T. Mossman (Eds.), Cell Imaging Techniques: methods and protocols (pp. 275-294). Totowa, New Jersey: Humana Press.

Item is

Files

show Files

Locators

show

Creators

show
hide
 Creators:
Hausmann, Michael, Author
Perner, Birgit, Author
Rapp, Alexander, Author
Wollweber, Leo, Author
Scherthan, Harry1, Author           
Greulich, Karl-Otto, Author
Affiliations:
1Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433549              

Content

show
hide
Free keywords: Near-field scanning optical microscopy; NSOM; applications in biology; cell surfaces; metaphase chromosomes; meiotic chromosomes
 Abstract: Light microscopy has proven to be one of the most versatile analytical tools in cell biology and cytogenetics. The growing spectrum of scientific knowledge demands a continuous improvement of the optical resolution of the instruments. In far-field light microscopy, the attainable resolution is dictated by the limit of diffraction, which, in practice, is about 250 nm for high-numerical-aperture objective lenses. Near-field scanning optical microscopy (NSOM) was the first technique that has overcome this limit up to about one order of magnitude. Typically, the resolution range below 100 nm is accessed for biological applications. Using appropriately designed scanning probes allows for obtaining an extremely small near-field light excitation volume (some tens of nanometers in diameter). Because of the reduction of background illumination, high contrast imaging becomes feasible for light transmission and fluorescence microscopy. The height of the scanning probe is controlled by atomic force interactions between the specimen surface and the probe tip. The control signal can be used for the production of a topographic (nonoptical) image that can be acquired simultaneously. In this chapter, the principle of NSOM is described with respect to biological applications. A brief overview of some requirements in biology and applications described in the literature are given. Practical advice is focused on instruments with aperture-type illumination probes. Preparation protocols focussing on NSOM of cell surfaces and chromosomes are presented.

Details

show
hide
Language(s): eng - English
 Dates: 2006-01-01
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: eDoc: 307652
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: Cell Imaging Techniques : methods and protocols
Source Genre: Book
 Creator(s):
Taatjes, Douglas J., Editor
Mossman, Brooke T., Editor
Affiliations:
-
Publ. Info: Totowa, New Jersey : Humana Press
Pages: - Volume / Issue: - Sequence Number: - Start / End Page: 275 - 294 Identifier: ISBN: 1-59259-993-1

Source 2

show
hide
Title: Methods in molecular biology
Source Genre: Series
 Creator(s):
Walker, John M., Editor
Affiliations:
-
Publ. Info: -
Pages: - Volume / Issue: 319 Sequence Number: - Start / End Page: - Identifier: -